Celerion
Clinical Research Coordinator
Celerion, Lincoln, Nebraska, United States, 68511
Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
We are seeking a
Clinical
Research Coordinator
to join our Lincoln, NE team!
This is a great opportunity for someone seeking a career change. Training is provided.
As a
Clinical Research Coordinator
you are responsible for oversight and conduct of clinical studies. You will ensure compliance, quality, and profitability of clinical studies. You respond to internal and external client issues, concerns, and requests by applying study management techniques and tools. In this role you should plan to work some evening and weekends.
Primary Responsibilities:
You are responsible for the overall management of Clinical Studies to include: on-time performance with defect-free execution, independently conducting bioequivalency and bioavailability studies, working with support divisions to ensure timelines are being met in clinical studies (i.e. recruiting, data management, statistics), organizing study initiation meetings to plan execution of study, facilitating study review meetings for pre-study, in-process and post study review, problem solving as needed during study conduct, meeting with clients as needed throughout study, and organizing study logistics and personnel. In addition, you will be present at critical events and dosings of study. You will build client relationships that result in additional business, you will craft and edit reports, respond to client issues, concerns and requests, adhere to milestone guidelines, and ensure profitability by maintaining profitability of team through a budgeting and expense control on a total and individual study basis.
Requirements
You will have a Bachelor's degree in a related discipline or BSN required. Celerion experience may be considered in lieu of degree in some situations.Industry experience and knowledge of medical terminology preferred.Demonstrated organizational, time management and multi-tasking skills requiredShown ability to handle multiple prioritiesExcellent oral and written communication skillsYou will work without close supervisionAbility to work flexible hours required for study conductYou will utilize customer service skillsClinical Research experience useful, but not required
Celerion Values: Integrity Trust Teamwork Respect
Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.
We are seeking a
Clinical
Research Coordinator
to join our Lincoln, NE team!
This is a great opportunity for someone seeking a career change. Training is provided.
As a
Clinical Research Coordinator
you are responsible for oversight and conduct of clinical studies. You will ensure compliance, quality, and profitability of clinical studies. You respond to internal and external client issues, concerns, and requests by applying study management techniques and tools. In this role you should plan to work some evening and weekends.
Primary Responsibilities:
You are responsible for the overall management of Clinical Studies to include: on-time performance with defect-free execution, independently conducting bioequivalency and bioavailability studies, working with support divisions to ensure timelines are being met in clinical studies (i.e. recruiting, data management, statistics), organizing study initiation meetings to plan execution of study, facilitating study review meetings for pre-study, in-process and post study review, problem solving as needed during study conduct, meeting with clients as needed throughout study, and organizing study logistics and personnel. In addition, you will be present at critical events and dosings of study. You will build client relationships that result in additional business, you will craft and edit reports, respond to client issues, concerns and requests, adhere to milestone guidelines, and ensure profitability by maintaining profitability of team through a budgeting and expense control on a total and individual study basis.
Requirements
You will have a Bachelor's degree in a related discipline or BSN required. Celerion experience may be considered in lieu of degree in some situations.Industry experience and knowledge of medical terminology preferred.Demonstrated organizational, time management and multi-tasking skills requiredShown ability to handle multiple prioritiesExcellent oral and written communication skillsYou will work without close supervisionAbility to work flexible hours required for study conductYou will utilize customer service skillsClinical Research experience useful, but not required
Celerion Values: Integrity Trust Teamwork Respect
Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.